State
73,495 recalls have nationwide distribution and so reach Arkansas. 5,543 additional recalls listed Arkansas specifically in their distribution scope.
Of the 5,543 recalls naming Arkansas we have scored against our rubric, 1,029 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,446 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,543 recalls whose distribution notice names Arkansas specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
NutraCap Labs LLC is recalling KO Nutrition Essential Health Tropical Fruit Punch 25oz jars because the product contains undeclared shellfish, which poses an allergic reaction risk to sensitive consumers.
NutraCap Labs LLC is recalling Genius Plus Focus Capsules 4ct packages due to undeclared milk. The product was distributed across 25 states and poses a risk to consumers with milk allergies.
NutraCap Labs LLC is recalling Mind Functions Brainology Capsules (132ct bottle) because the product contains undeclared milk, a common allergen.
NutraCap Labs LLC is recalling SRS Nutra LTD Physio Flex Joint Support Capsules due to undeclared shellfish in the product. Consumers with shellfish allergies should not use this product.
NutraCap Labs LLC is recalling AIOS Synergy for Men Capsules (120ct bottles) because the product contains undeclared milk. The recall affects lot 2102130 with an expiration date of 02/2023, distributed across 25 states.
NutraCap Labs LLC is recalling Nutra Black Recovery Chocolate 128oz jars (Lot #2001230, exp. 01/2022) distributed across 25 states because the product contains undeclared shellfish, which poses a risk to consumers with shellfish allergies.
NutraCap Labs LLC is recalling DH Nutra Define Thermogenic Capsules because the product contains undeclared milk, a common allergen that poses a risk to consumers with milk allergies.
NutraCap Labs LLC is recalling Unlocked Supplements Sana Capsules (90ct bottles, UPC 6 79360 63826 2, Lot #2004014) because the product contains undeclared milk, a major allergen. The product was distributed across 25 states.
Mass Nutraceuticals Brain Food Capsules are being recalled because they contain undeclared milk. The product was distributed across 25 states and may pose a risk to consumers with milk allergies.
NutraCap Labs LLC is recalling Adrenalyne Razzled Up Blue Raspberry 25oz jars because the product contains undeclared shellfish, which poses a risk to consumers with shellfish allergies.
NutraCap Labs LLC is recalling Premier Dynamic Nutrition Kinetic Greens Green Lemonade 25oz jars because they contain undeclared milk, a common allergen. The product was distributed across 25 states.
NutraCap Labs LLC is recalling Bic Nutrition Olympus Fruit Punch 64oz bottles due to undeclared shellfish. The product was distributed across 25 states and poses a risk to consumers with shellfish allergies.
NutraCap Labs LLC is recalling Macro Supps ONE Greens Strawberry Kiwi 25oz jars because the product contains undeclared milk, which poses a hazard to consumers with milk allergies.
NutraCap Labs LLC is recalling Global Link ShredFX Popsicle 16oz jars because the product contains undeclared milk. Consumers with milk allergies or sensitivities are at risk.
NutraCap Labs LLC is recalling Black Magic Brain Waves Capsules 120ct bottles because the product contains undeclared milk. Consumers with milk allergies or sensitivities are at risk.
NutraCap Labs LLC is recalling TM Nutrition Restoration Pineapple 19oz jars because the product contains undeclared milk, a common allergen. The recall affects 80,169 units distributed across 25 states.
Philips wireless footswitches used with Allura Xper and Azurion X-ray systems may experience connection issues that interrupt fluoroscopic imaging during patient procedures. The recall affects 1,971 systems distributed worldwide.
Medtronic is recalling approximately 6,653 Custom Perfusion kits used in cardiac procedures because they were labeled as non-pyrogenic without completing required endotoxin testing.
Siemens SOMATOM Edge Plus CT systems running software version VB20_SP5 may produce degraded head images, potentially leading to patient misdiagnosis.
Mushie & Co is recalling about 333,725 FRIGG Silicone Pacifiers because the silicone nipple can detach from the plastic shield, posing a choking hazard. Eight detachments have been reported in the U.S. with no injuries.
Haag-Streit OCT-Camera devices with automatic laser shut-off malfunction may fail to recognize when the laser is safely switched off, posing a potential safety risk.
Childrensalon is recalling about 180 children's sleepwear garments that fail to meet U.S. flammability standards, posing a burn injury risk. Consumers should stop using the garments immediately and contact Childrensalon for return instructions.
Siemens SOMATOM Confidence CT scanners with software version VB20_SP5 may experience degraded head image quality, creating a potential risk of misdiagnosis. The recall affects 108 units distributed nationwide.
Canon Medical's flat panel detectors used in Alphenix surgical systems may display abnormal horizontal stripes and fail to recover by restarting, potentially causing operators to work without proper visual guidance during procedures.
DePuy Orthopaedics is recalling GLOBAL UNITE STD STEM orthopedic implants due to undersized spigot bore diameter that may prevent proper removal during revision surgery, risking surgical delay and bone damage.